Anti-Inflammatory Metabolites in the Pathogenesis of Bacterial Infection
Overview
Infectious Diseases
Microbiology
Authors
Affiliations
Host and pathogen metabolism have a major impact on the outcome of infection. The microenvironment consisting of immune and stromal cells drives bacterial proliferation and adaptation, while also shaping the activity of the immune system. The abundant metabolites itaconate and adenosine are classified as anti-inflammatory, as they help to contain the local damage associated with inflammation, oxidants and proteases. A growing literature details the many roles of these immunometabolites in the pathogenesis of infection and their diverse functions in specific tissues. Some bacteria, notably , actively metabolize these compounds, others, such as respond by altering their own metabolic programs selecting for optimal fitness. For most of the model systems studied to date, these immunometabolites promote a milieu of tolerance, limiting local immune clearance mechanisms, along with promoting bacterial adaptation. The generation of metabolites such as adenosine and itaconate can be host protective. In the setting of acute inflammation, these compounds also represent potential therapeutic targets to prevent infection.
Challenges and limitations in using bacterial metabolites as immunomodulators.
Saravanan C, Gopinath N, Ganesan R, Thirumurugan D Front Cell Infect Microbiol. 2025; 15:1535394.
PMID: 39944722 PMC: 11814176. DOI: 10.3389/fcimb.2025.1535394.
Efficacy of Ambroxol Combined with Loquat Syrup on Bacterial Pneumonia in Mice.
Li C, Chen Z, Shi J, Zheng X J Inflamm Res. 2024; 17:10107-10117.
PMID: 39639928 PMC: 11619114. DOI: 10.2147/JIR.S478655.
Suppressing neutrophil itaconate production attenuates Mycoplasma pneumoniae pneumonia.
Wang C, Wen J, Yan Z, Zhou Y, Gong Z, Luo Y PLoS Pathog. 2024; 20(11):e1012614.
PMID: 39499730 PMC: 11567624. DOI: 10.1371/journal.ppat.1012614.
Gautam H, Shaik N, Banaganapalli B, Popowich S, Subhasinghe I, Ayalew L J Anim Sci Biotechnol. 2024; 15(1):144.
PMID: 39487547 PMC: 11531110. DOI: 10.1186/s40104-024-01105-5.
Singh S, Singh P, Ahmad Z, Das S, Foretz M, Viollet B J Immunol. 2024; 213(11):1656-1665.
PMID: 39413004 PMC: 11573643. DOI: 10.4049/jimmunol.2400282.